Composition based on glycerol ether/polyol mixtures

ABSTRACT

The invention relates to compositions which comprise one or more glycerol ethers together with one or more diol/diols and/or polyol/polyols. As a result, as well as good microbicidal effectiveness, whitening is reduced or avoided, drying-out of the skin is prevented, the moisture content is regulated and the skin is regreased to an adequate extent.

The invention relates to compositions which, besides one or moreglycerol ethers, comprise one or more polyols.

Alcohols, polyols and also glycerol ethers in general are used widely inthe field of cosmetic, pharmaceutical, dermatological and also technicalproducts. Criteria here are often antimicrobial effectiveness, andmaterial and skin compatibility.

There is a constant need for compositions with improved properties, withapplications to the skin and the feel which arises following applicationof the corresponding product, and the resulting appearance alsoincreasingly playing a greater role. Often, following use ofcorresponding products, an unpleasant feeling of dryness, a feeling ofstickiness and/or even an undesired visible residue presents itself,depending on the composition.

At a time of increasing hygiene awareness on the part of the consumerand increased use of cosmetic cleansing and care products, such as, forexample, soaps, creams, deodorant products, shower and bathpreparations, the increased use of alcohol-, soap- andsurfactant-containing products on the skin also often results in theabove-stated unpleasant accompanying phenomena.

The object of the invention is therefore to provide compositions withmicrobicidal and/or preservative and/or cosmetic effect and/ordermatological effect and/or pharmaceutical effect which do not exhibit,or exhibit to a reduced degree, the above-stated disadvantages andunpleasant accompanying phenomena. In this connection, while achieving agood or improved microbicidal and simultaneously regreasing effect it isnecessary to prevent or restrict so-called “whitening”.

This object is achieved through compositions which comprise one or moreglycerol ethers together with one or more diols and/or polyols.

Preferred embodiments of the invention are subject matter of thedependent claims.

The invention also covers the use of such compositions in suitableproducts for achieving the effects desired in each case.

The glycerol ethers which can be used according to the invention arepreferably mono-, di- or trialkyl, -aralkyl, -alkylaryl or -arylglycerol ethers having, if present, in each case (also independently ofone another) saturated or unsaturated, branched or unbranchedC₁-C₂₄-alkyl groups, and, if present, C₆-C₁₀-aryl groups.

The glycerol ethers according to the invention have the formula

and are preferably glycerol monoalkyl ethers with the formula

In the above formulae, R, in each case independently of the others, ispreferably a straight- or branched-chain, saturated or unsaturatedalkyl, aralkyl or alkylaryl group having preferably 6 to 18, inparticular 7 to 12 and preferably 8 to 12, particularly preferably 8,carbon atoms in the alkyl group.

These include, for example, the preferred 1-octadecyl glycerol ethers(also known as batyl alcohol), 1-hexadecyl glycerol ether (also known aschimyl alcohol), 1-(9-octadecenyl)glycerol ether (also known as selachylalcohol), 1-dodecyl glycerol ether, 1-decyl glycerol ether,1-(2-propylheptyl)glycerol ether, 1-octyl glycerol ether and1-(2-ethylhexyl)glycerol ether (also referred to as3-((2-ethylhexyl)oxy)-1,2-propanediol, where 1-(2-ethylhexyl)glycerolether is particularly preferred.

It is also possible to use mixtures of glycerol ethers according to theinvention.

The glycerol ethers used according to the invention, in particular theglycerol monoalkyl ethers, are colour- and odour-neutral compounds whichcan be produced in chemically pure form.

Derivatives with an alkyl radical having up to 9 carbon atoms which areliquid at room temperature can be incorporated into productsparticularly easily and are therefore preferred.

Of particular advantage is the greater chemical stability of theglycerol monoalkyl ethers compared to fatty acid esters, e.g. mono- anddiglycerides. On account of their ether structure, they can also be usedin the alkaline sector. This is particularly advantageous for use inliquid soaps where, at high pH values and a large water content,hydrolysis of the glycerides results with release of fatty acids, whichmanifests itself, inter alia, in a poor low-temperature stability of thecorresponding products. Enzymatic cleavage with release of fatty acids,which can arise in the case of the glycerides, is also not to be fearedin the case of the glycerol ethers.

The diols used according to the invention include alkanediols having 4to 16 carbon atoms, preferably 6 to 10 carbon atoms, preferably 6 to 8carbon atoms, in the alkylene chain, such as butylene glycols,pentanediols, hexanediols, heptanediols, octanediols and decanediols, inparticular 1,2-butanediol, 1,2-pentanediol, 1,2-hexanediol,1,2-heptanediol, 1,2-octanediol, and mixtures thereof, such as, forexample, a mixture of 1,2-hexanediol and 1,2-octanediol.

The mixing ratio in mixtures of diols is arbitrary here and can be, forexample, 10:1 to 1:10, preferably 5:1 to 1:5, in particular 2:1 to 1:2,particularly preferably 1:1.

Polyols used according to the invention include triols, such as glyceroland sugar alcohols, such as threitol, glucitol, sorbitol and inositol,or mixtures thereof.

Particular preference is given to the diols 1,2-hexanediol,1,2-octanediol, a mixture of the same and the polyol glycerol.

The mixing ratio in mixtures of polyols is here again arbitrary and canbe, for example, 20:1 to 1:20, preferably 10:1 to 1:10, more preferably5:1 to 1:5 and in particular 2:1 to 1:2.

The compositions according to the invention comprise at least oneglycerol ether in an amount of from 0.01 to 30 or 40% by weight,preferably 0.05 to 10% by weight, in particular 0.1 to 5% by weight,preferably 0.5 to 2 or 3% by weight.

In addition, they comprise at least one diol or polyol in an amount offrom 0.01 to 99.99% by weight, preferably 0.05 to 40% by weight, inparticular 0.1 to 10% by weight, preferably 0.5 to 5 or 8% by weight.

The use concentration of the components also varies as a function of thetype and concentration of the other constituents, such as thewashing-active substances and the further additives, and also dependingon the strength of the desired effect, in particular the microbicidal,anti-whitening and regressing effects.

Excluded from the present invention are aftershave formulations whichcomprise 1-(2-ethylhexyl)glycerol ether, glycerol and ethanol, and alsoday creams which comprise 1-dodecyl glycerol ether and glycerol.

Preferred compositions according to the invention comprise:

-   -   glycerol monoalkyl ethers, in particular        1-(2-ethylhexyl)glycerol ether, together with 1,2-hexanediol,        1,2-octanediol, a mixture of 1,2-hexanediol and 1,2-octanediol,        or    -   glycerol monoalkyl ethers, in particular        1-(2-ethylhexyl)glycerol ether, together with glycerol.

The compositions according to the invention are antimicrobially ormicrobicidally effective and can be used in cosmetic, pharmaceutical,dermatological and also technical products (such as, for example,cooling lubricants) for deactivating microorganisms such as bacteria,yeasts, fungi and viruses, including microorganisms which arecomparatively difficult to deactivate, such as mycobacteria, Mallaseziafurfur, Propionibacterium acnes, and odour-causing microbes.

In particular, application to the skin is possible here withoutproblems, something which is also due to the excellent regressingproperties, the imparting of a very pleasant feel on the skin and also avery good spreadability on the skin.

When applying cosmetic O/W emulsions (e.g. creams, lotions) to the skin,a troublesome effect is often observed, which is referred to aswhitening effect. When using the compositions according to theinvention, the troublesome “whitening” is advantageously avoided orconsiderably reduced.

Besides the glycerol ether(s) and diol(s) and/or polyol(s), thecompositions according to the invention can also comprise suitable andoptional additives, although these are not required for the preparationof the compositions according to the invention and can therefore also beomitted according to the most general embodiment of the invention.

Suitable additives are, for example, aliphatic alcohols, such asethanol, isopropanol, n-propanol and fatty alcohols, aromatic alcohols,such as benzyl alcohol, phenethyl alcohol, phenylpropanols,phenoxyethanol, phenoxypropanols, and propylene glycol monobutyl ether,butyl diglycol, fatty alcohol esters and fatty acid esters. However,nonionic and ionic surfactants, glucosides and other customaryauxiliaries, such as thickeners, emulsifiers, preservatives, dispersionauxiliaries etc. can also be used. Phenoxyethanol is a preferredadditive here. Further functional additives are, for example, complexingagents and solubility promoters, which can be used particularly in thepreparation of concentrates.

The compositions are preferably aqueous, aqueous/alcoholic or alcoholic.They can also be present in the form of a concentrate, a low-viscositythin-liquid or higher-viscosity but flowable composition, a cream, salveor paste, or an emulsion (W/o or O/W).

The application temperature can range from ambient temperature or roomtemperature (20° C.) to, for example, 30° C., 37° C. or 50° C. or more,e.g. when used in masks.

The other additives of the composition are selected depending on thedesired consistency or the desired field of use.

The compositions according to the invention can be in the form of anaqueous and/or alcoholic solution, cream or emulsion in which, inparticular, a mixture with surface-active substances, in particularemulsifiers or surfactants, and/or other additives is present.

The compositions according to the invention can be used in particular inskincare products from the cosmetic and near-cosmetic sector. Theseinclude, for example, cleaning and care products, such as solid orliquid soaps, shower baths, shower gels, foam baths, shampoos, washinglotions, day creams, moisturizing creams, O/W or W/O care creams, O/W orW/O care emulsions, aftershave solutions or emulsions and handdishwashing compositions.

The regreasing of the skin and the imparting of a pleasant feel on theskin and feeling of smoothness and the avoidance of stickiness followinguse also takes place surprisingly well through the combination of theglycerol ethers and di- and/or polyols present according to theinvention. A silky, velvety, soft feel is produced in contrast to a waxyor oily feel. The spreadability and the ability to absorb on or in theskin is also improved.

To improve the stability, the organoleptic properties and to prevent orreduce the formation of undesired degradation products, it isparticularly preferred to add stabilizers and/or antioxidants to thecompositions according to the invention.

Examples of stabilizers and/or antioxidants are

-   -   low-temperature stabilizers, such as lower alcohols, e.g.        ethanol, propanols, glycols, e.g. 1,2-propylene glycol, glycol        ethers,    -   phenol compounds, such as 3-tert-butyl-4-hydroxyanisole,        2,6-di-tert-butyl-p-cresol, dodecyl gallate, pyrogallate,        tocopherol (e.g. vitamin E), and its derivatives (e.g. vitamin E        acetate), preferably vitamin E and its derivative, particularly        preferably vitamin E.

The stabilizers and/or antioxidants can be present in the compositionsin a concentration of from 0.0001% by weight to 5% by weight, preferably0.001% by weight to 0.5% by weight, particularly preferably 0.01% byweight to 0.1% by weight, e.g. 0.015% by weight.

In addition, a good deodorizing effect and an increase in thepreservative effect of other preservatives arises.

The compositions according to the invention can be used as concentrateor dilute use solutions. Suitable glycerol ether concentrations forconcentrates are, for example, 10 to 40% by weight, in particular 15 to30% by weight. Suitable glycerol ether concentrations for dilute usesolutions are, for example, 0.1 to 5% by weight, preferably 1 to 3.0% byweight, or preferably 0.5 to 2.0% by weight.

The invention is further illustrated below by examples.

EXAMPLES Example 1 Cream—Sensory Effect

An exemplary product according to the invention is a cream B with thefollowing composition:

% by wt. Arachidyl alcohol/behenyl alcohol/arachidyl glucoside 5(standard commercial mixture Montanov ® 202) Cetearyl octanoate 20(Lanol ® 1688) 1-(2-Ethylhexyl) glycerol ether 1 (Sensiva ® SC 50)Polyacrylate-13/polyisobutene/polysorbate 20 0.2 (standard commercialmixture Sepiplus ® 400) Water (demineralized) 64.3 Glycerol (85%strength) 9.4 (corresponds to 8% by weight of glycerol as ingredient)Benzyl alcohol/methylchloroisothiazolinone/methyl- 0.1 isothiazolinone(standard commercial mixture Euxyl ® K 100) 100

The comparison product used was a cream A with the same composition butin which the 1% by weight of glycerol ether had been replaced by 1% byweight of water.

The two creams A and B are assessed here by a group of 22 subjects whichhave applied the particular product to the skin. The creams were eachapplied once per day to the test area (in each case one and always thesame area on the inside of the forearm) in circular rubbing movements.The test time was 3 days. In each case suitable and in each case thesame amounts of creams A and B were used. The sensitivity was assessedimmediately and 3 minutes afterwards using those fingers which were notinvolved in the rubbing in. The sensitivity was assessed in each casethree times at each time point.

The sensory results in the case of these two creams A and B were asfollows:

Stickiness:

The stickiness was evaluated directly after application (t=0) and 3minutes after application (t=3 min). The average values are given. Theevaluation scale ranged from 0 to 5. Considerable stickiness wasevaluated as 5. In the case of the absence of stickiness, a 0 wasawarded.

t = 0 t = 3 min Cream A: 2.8 2.8 Cream B: 2.0 1.9(All of the values were between 1 and 4).Whitening:

The whitening was assessed directly after application. Again, theaverage values are given. The evaluation scale ranged from 0 to 5.Considerable whitening was evaluated as 5. In the absence of whitening,a 0 was awarded.

Cream A: 2.8 Cream B: 1.9(All of the values were between 1 and 4).Ability to Absorb:

The ability to absorb was assessed directly after application (t=0) and3 minutes after application (t=3 min). The average values are given. Theevaluation scale ranged from 0 to 5. Slow absorption was evaluated as 5.Rapid absorption was evaluated as 0.

t = 0 t = 3 min Cream A: 3.1 3.0 Cream B: 2.2 2.1(All of the values were between 1 and 5).Pleasant Feel on the Skin:

It was assessed how pleasant the feel on the skin was perceived 3minutes after application. Again, the average values are given. Theevaluation scale ranged from 0 to 5. An unpleasant feel on the skin wasevaluated as 5. A pleasant feel on the skin was evaluated as 0.

Cream A: 2.5 Cream B: 1.8(All of the values were between 1 and 4 in the case of cream A, andbetween 1 and 3 in the case of cream B).Greasy Skin Feel:

It was assessed how greasy the feel on the skin was perceived 3 minutesafter application. Again, the average values are given. The evaluationscale ranged from 0 to 5. A greasy feel on the skin was evaluated as 5.A nongreasy feel on the skin was evaluated as 0.

Cream A: 3.1 Cream B: 2.3(All of the values were between 1 and 5 in the case of cream A, andbetween 1 and 4 in the case of cream B).Feeling of Smoothness:

It was assessed how the smoothness of the skin was perceived 3 minutesafter application. Again, the average values are given. The evaluationscale ranged from 0 to 5. A harsh feel on the skin was evaluated as 5. Asmooth feel on the skin was evaluated as 0.

Cream A: 2.8 Cream B: 2.1(All of the values were between 1 and 5).

In summary, the following picture emerged with regard to the sensoryproperties:

The subjects established a clear difference between the two creamformulations.

Cream B with the glycerol ether/diol combination according to theinvention left behind a clearly detectable pleasant feel on the skinfollowing application, which was described with the adjectives

-   -   velvety    -   smooth    -   supple.

As regards the feel on the skin following application of the comparisonformulation A without the glycerol ether, the following statements weremade:

-   -   dry    -   rough    -   harsh.

It was particularly advantageously additionally established that theskin following application of the cream containing glycerol ether feltneither greasy nor sticky.

For comparison, composition C, which comprised only the glycerol etherhut no glycerol, and composition D, which comprised neither glycerolether (3% by weight of glycerol ether replaced by water) nor glycerol,were also investigated.

% by wt. Arachidyl alcohol/behenyl alcohol/arachidyl glucoside 5(standard commercial mixture Montanov ® 202) Cetearyl octanoate 20(Lanol ® 1688) Cetylstearyl alcohol 1 1-(2-Ethylhexyl) glycerol ether 3(or 0) (Sensiva ® SC 50) Polyacrylate-13/polyisobutene/polysorbate 200.2 (standard commercial mixture Sepiplus ® 400) Water (completelydemineralized) 70.7 (or 73.7) Benzylalcohol/methylchloroisothiazolinone/methyl- 0.1 isothiazolinone(standard commercial mixture Euxyl ® K 100) 100

The result of the assessment was that the achieved effects do notmeasure up to the skincare effects achieved above for the combination ofthe glycerol ether/glycerol neither in the case of composition D nor inthe case of composition C (with a content of 3.0% by weight of glycerolether).

Example 2 Microbicidal Effect

Besides the sensory evaluation, the microbicidal effect of a compositionaccording to the invention was also investigated.

A quantitative suspension experiment was carried out in accordance withDGHM against Microbacterium terrae.

Inactivator: Phosphate buffer+THS−NT

Starting germ count: 3.4×10⁹

In each case, the Rf values are given.

The following compositions E, F and G were tested, the data being givenin % by weight:

Composition: E F G 1-(2-Ethylhexyl) glycerol ether 0.1 0.11,2-Hexanediol/1,2-octanediol (1:1) 0.6 0.6 0.6 Water (completelydemineralized) 99.3 99.4 99.9

Compositions F and G do not belong to the invention and serve forcomparison purposes.

The resulting Rf values are given in the table below.

Contact time 15 min 30 min 60 min E 0 1.76 3.07 F 0 0 0 G 0 0 0Result:

The combination of glycerol ether with a diol mixture (E) has a bettereffect, at a comparable concentration, than the diol mixture (F) on itsown and the glycerol ether (G) on its own. This gives rise to aconsiderable increase in the effect for a diol mixture (F) as a resultof the addition of glycerol ether (G) which, on account of the lack ofan effect of the glycerol ether on its own, could not be expected.Synergism is present.

Example 3 Microbicidal Effect

A composition was tested which comprised 30% by weight of1-(2-ethylhexyl)glycerol ether and 70% by weight of 1,2-octanediol.

It exhibits good results with regard to skin moisture, deodorizingeffect and increase in the preservative effect of other preservatives,such as, for example, of parabens, in particular methyl paraben, orphenoxyethanol e.g. towards Aspergillus niger, Candida albicans,Staphylococcus aureus, Pseudomonas aeruginose and Eschirichia coli.

1. A method of providing a sensory effect on the skin comprising:applying, once per day to the skin, a day cream which comprises1-(2-ethylhexyl) glycerol ether, 1,2-octanediol, and one or more polyolsselected from the group consisting of glycerol, glucitol, sorbitol andinositol, the application being in circular rubbing movements.
 2. Themethod according to claim 1, wherein the day cream further comprises oneor more diols, where the diol/diols is/are an alkanediol having 4 to 16carbon atoms in the alkylene chain.
 3. The method according to claim 2,wherein the mixing ratio of a mixture of diols is 10:1 to 1:10.
 4. Themethod according to claim 1, wherein the day cream comprises a mixtureof two or more polyols.
 5. The method according to claim 4, wherein themixing ratio of the mixture of polyols is 20:1 to 1:20.
 6. The methodaccording to claim 1, wherein the day cream further comprises1,2-hexanediol and/or glycerol.
 7. The method according to claim 1,wherein the day cream comprises a mixture of one or more diols and oneor more polyols, and the mixing ratio of a mixture of diol(s) andpolyol(s) is 10:1 to 1:10.
 8. The method according to claim 1, whereinthe day cream comprises at least one glycerol ether in an amount of from0.01 to 30 or 40% by weight, and comprises at least one diol or polyolin an amount of from 0.01 to 99.99% by weight.
 9. The method accordingto claim 2, wherein the mixing ratio of a mixture of diols is 5:1 to1:5.
 10. The method according to claim 2, wherein the mixing ratio of amixture of diols is 2:1 to 1:2.
 11. The method according to claim 2,wherein the mixing ratio of a mixture of diols is 1:1.
 12. The methodaccording to claim 4, wherein the mixing ratio of the mixture of polyolsis 10:1 to 1:10.
 13. The method according to claim 4, wherein the mixingratio of the mixture of polyols is 5:1 to 1:5.
 14. The method accordingto claim 4, wherein the mixing ratio of the mixture of polyols is 2:1 to1:2.
 15. The method according to claim 1, wherein the day cream furthercomprises 1,2-hexanediol, and the 1,2-hexanediol and 1,2-octanediol arepresent in a mixing ratio of from 10:1 to 1:10, and/or glycerol.
 16. Themethod according to claim 1, wherein the day cream further comprises1,2-hexanediol, and the 1,2-hexanediol and 1,2-octanediol are present ina mixing ratio of from 5:1 to 1:5, and or glycerol.
 17. The methodaccording to claim 1, wherein the day cream comprises 1,2-hexanediol,and the 1,2-hexanediol and 1,2-octanediol are present in a mixing ratioof from 2:1 to 1:2, and or glycerol.
 18. A method of providing a sensoryeffect on the skin comprising: applying to the skin a day creamcomprising 1-(2-ethylhexyl) glycerol ether and 1,2-octanediol and one ormore polyols selected from the group consisting of glycerol, glucitol,sorbitol and inositol.